Allele Registry

Canonical Allele Identifier: PA2826601048

Gene: DNM1L HGNC NCBI

ClinVar RCV:

RCV000006386

ClinVar Variation:

6015

HGVS (amino-acid)	Matching Registered Transcripts
NP_001265395.1:p.Ala192Asp	CA117911 NM_001278466.2:c.575C>A